Furanochromone
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| Names | |
|---|---|
| IUPAC name
5H-Furo[3,2-g]chromen-5-one | |
| Identifiers | |
67777-61-1  | |
| ChemSpider | 114232 |
| |
| Jmol-3D images | Image |
| PubChem | 128913 |
| |
| Properties | |
| Molecular formula |
C11H6O3 |
| Molar mass | 186.16 g·mol−1 |
| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Infobox references | |
Furanochromone is a chemical compound which is a derivative of chromone (1,4-benzopyrone) and furan.[1]
Some chemical derivatives of furanochromone show strong interaction with DNA.[2] Furanochromones can be produced in callus cultures of Ammi visnaga[3] or in Pimpinella monoica.[4]
References
- ↑ Pereira, David M.; Valentão, Patrícia; Pereira, José A.; Andrade, Paula B. (2009). "Phenolics: From Chemistry to Biology". Molecules 14 (6): 2202. doi:10.3390/molecules14062202.
- ↑ Niccolai, Neri; Bovalini, Lucia; Martelli, Paola (1986). "The mechanisms of interaction between furanochromones and dna". Biophysical Chemistry 24 (3): 217–20. doi:10.1016/0301-4622(86)85027-X. PMID 3768467.
- ↑ Krolicka A., Staniszewska I., Malinski E., Szafranek J. and Łojkowska E. (2003). "Stimulation of furanochromone accumulation in callus cultures of Ammi visnaga L. by addition of elicitors". Pharmazie 58 (8): 590–592. PMID 12967041.
- ↑ D. L. Luthria and A. Banerji (1994). "Biosynthesis of furanochromones in Pimpinella monoica" (PDF). Journal of Chemical Sciences 106 (5): 1149–1156. doi:10.1007/BF02841922.
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